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Researchers find how biological markers predict risk of postpartum depression

by Vaishali Sharma
Davis said he'll be interested to see if these subtypes of experiences are applicable in the clinical setting, where psilocybin-assisted therapy is being studied at Ohio State for the treatment of post-traumatic stress disorder in military veterans. "Finding the variety of other outcomes that these subtypes might be related to is an interesting next step," he said. "These could include adaptive or functional outcomes in people's quality of life or well-being, or a better understanding of their life's purpose or relationships."

A group of scientists revealed that cell communication is disrupted in pregnant women who suffer postpartum depression (PPD) after giving birth.

The findings of a study headed by Johns Hopkins Medicine were published in the journal Molecular Psychiatry. Premature deliveries, gestational diabetes, toxic maternal high blood pressure, and other pregnancy-related disorders have previously been linked to changes in extracellular RNA transmission, a recently discovered cell signalling pathway. The current study’s researchers studied maternal blood to see if there were any noticeable alterations in this extracellular communication pathway during PPD.

The extracellular RNA communication changes identified in the study suggest that women who develop PPD are unable to efficiently remove aging and defective cell components. This process, called autophagy, is also known to malfunction in the brain of patients with Alzheimer’s and Parkinson’s disease. “Potentially, postpartum depression could be treated using certain Alzheimer’s and Parkinson’s disease medications that induce autophagy,” says Sarven Sabunciyan, Ph.D., an assistant professor of pediatrics at the Johns Hopkins University School of Medicine and the paper’s senior author.

One in nine new mothers has postpartum depression, a condition marked by periods of sadness, loneliness and inability to care for their newborns that last longer than two weeks. “With postpartum depression, there are many potential negative outcomes, such as a high rate of suicide among mothers or a disruption in the baby’s cognitive, emotional and social development,” says Sabunciyan. “If we could identify mothers who may be more at risk ahead of the birth, we might prevent these adverse events.”

Efforts have been underway for decades to identify genetic or other biological markers for PPD.

In the new study, the research team specifically investigated the messenger RNA (mRNA) content of extracellular vesicles (EVs) — fatty sacs of genetic material that is essential to communication among cells. During pregnancy, Sabunciyan says, this communication system ramps up to address needs for embryo implantation and growth. A mother’s placenta also releases RNA vital for immune system development that protects the growing fetus from viruses.

Sabunciyan, a neuroscientist at Johns Hopkins Children’s Center whose work focuses on the root causes of psychiatric disorders, says the research team collected blood samples from 42 women who were pregnant and were seen at The Johns Hopkins Hospital.

Newly developed sequencing and computational analysis methods were used to measure the level of thousands of different mRNAs that are packaged into EVs in the blood of 14 participants during the second and third trimester of pregnancy and up to six months after giving birth. Seven of the participants were diagnosed with postpartum depression after childbirth, receiving a score of 13 or above on the Edinburgh Postnatal Depression Scale (a standard tool to identify women with the condition). None of these women had signs of depression during pregnancy.

The mRNA levels identified to change the most robustly in participants who had PPD using this analysis were then measured in the blood of an additional 28 women during pregnancy. Fourteen of these women were diagnosed with PPD and five of them exhibited signs of depression during pregnancy. The changes in mRNA levels identified in those who developed PPD in the first set of 14 participants, replicated in the second group of 28 women, confirming the validity of the sequencing findings. Of the 42 women in the study, 34 were white, four were Asian or Pacific Islander, two were Black and two identified as another race. All were in their late 20s or early 30s, and had live births.

The research team says this analysis revealed that extracellular RNA communication levels during pregnancy and the postpartum period were “extensively altered” in women who developed postpartum depression. The researchers found that the level of 2,449 mRNAs changed (1,010 increased and 1,439 decreased) between those who went on to develop PPD compared with those who did not. On average, there was nearly a twofold difference in individual mRNA levels between the two groups. The vast majority of these changes occurred during the pregnancy instead of the postpartum period.

The researchers also discovered that EV mRNA levels associated with autophagy were decreased in women who later developed PPD — meaning the cells were not cleaning out excessive, damaged or defective parts. In addition, they found that EV mRNAs associated with PPD originated from white blood cells known as monocytes and macrophages.

The researchers caution that their study was limited by small numbers and a lack of racial diversity. But they say if further studies confirm the findings, they could potentially develop a blood test that can identify women who are pregnant who are at risk for developing PPD after delivery. The research may also advance development of therapies for PPD.

“If we can identify those at risk early, and get them into proper treatment, we’re likely to be able to prevent a lot of serious effects of postpartum depression,” Sabunciyan says.

Also Read: Social media usage associated with depression: Research

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